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dc.contributor.authorLiu, hongjun
dc.contributor.authorGrendal, Ola Gjønnes
dc.contributor.authorSkjærvø, Susanne Linn
dc.contributor.authorDalod, Antoine Robert Marie
dc.contributor.authorvan Beek, Wouter
dc.contributor.authorsekkat, abderrahime
dc.contributor.authorEinarsrud, Mari-Ann
dc.contributor.authormunoz-Rojas, David
dc.date.accessioned2020-09-29T07:02:22Z
dc.date.available2020-09-29T07:02:22Z
dc.date.created2020-09-22T15:58:21Z
dc.date.issued2020
dc.identifier.citationCrystal Growth & Design. 2020, 20 4264-4272.en_US
dc.identifier.issn1528-7483
dc.identifier.urihttps://hdl.handle.net/11250/2680097
dc.description.abstractAgCuO2 is an interesting semiconductor oxide with appealing optical and electronic properties. While the oxide has been synthesized in bulk by different approaches, no study on the formation mechanism has been carried out to date. We present an in situ time-resolved X-ray diffraction study of the hydrothermal synthesis of AgCuO2 from AgO and CuO. The effects of reaction pH and temperature on the reaction pathways and products have been studied. While pH is a key parameter for the successful synthesis of AgCuO2, temperature affects mainly the reaction kinetics. A reaction pathway is proposed that involves a series of dissolution-precipitation reactions, mediated by Cu and Ag hydroxy complexes. Finally, we have compared different approaches to obtain the reaction activation energy, which was calculated to be 70.6±5.1 kJ/mol. Nevertheless, our results show that new models need to be developed for the type of reaction presented here.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.titleReaction pathway of the hydrothermal synthesis of AgCuO2 from in situ time-resolved X-ray diffractionen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionacceptedVersionen_US
dc.source.pagenumber4264-4272en_US
dc.source.volume20en_US
dc.source.journalCrystal Growth & Designen_US
dc.identifier.doi10.1021/acs.cgd.9b01516
dc.identifier.cristin1832226
dc.relation.projectNorges forskningsråd: 250403en_US
dc.description.localcodeLocked until 27.4.2021 due to copyright restrictions. This document is the Accepted Manuscript version of a Published Work that appeared in final form in [JournalTitle], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.cgd.9b01516en_US
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode2


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